ClinVar Miner

List of variants in gene IL7R reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002185.5(IL7R):c.*1238A>T rs9292617 0.72701
NM_002185.5(IL7R):c.*1661G>A rs7716064 0.72649
NM_002185.5(IL7R):c.412G>A (p.Val138Ile) rs1494555 0.72524
NM_002185.5(IL7R):c.*2339T>C rs6451231 0.72445
NM_002185.5(IL7R):c.82+16G>C rs1353252 0.71907
NM_002185.5(IL7R):c.197T>C (p.Ile66Thr) rs1494558 0.68368
NM_002185.5(IL7R):c.*917G>A rs10063294 0.58961
NM_002185.5(IL7R):c.801-21A>T rs987106 0.53084
NM_002185.5(IL7R):c.*3007A>G rs700179 0.31973
NM_002185.5(IL7R):c.*2841T>C rs1053496 0.31938
NM_002185.5(IL7R):c.*1326A>G rs10491434 0.31937
NM_002185.5(IL7R):c.1066A>G (p.Ile356Val) rs3194051 0.28365
NM_002185.5(IL7R):c.*2507C>T rs6881270 0.24668
NM_002185.5(IL7R):c.731C>T (p.Thr244Ile) rs6897932 0.21045
NM_002185.5(IL7R):c.*3015A>G rs1862632 0.13303
NM_002185.5(IL7R):c.495C>T (p.His165=) rs2228141 0.13289
NM_002185.5(IL7R):c.*1552G>A rs10053847 0.13273
NM_002185.5(IL7R):c.*2547G>A rs13167136 0.13265
NM_002185.5(IL7R):c.*1924G>A rs9292618 0.13252
NM_002185.5(IL7R):c.*2995G>A rs72742450 0.04632
NM_002185.5(IL7R):c.561G>A (p.Lys187=) rs11567764 0.03877
NM_002185.5(IL7R):c.538-14A>C rs11567763 0.03352
NM_002185.5(IL7R):c.*1171G>A rs16902514 0.02323
NM_002185.5(IL7R):c.*2454T>A rs6862072 0.01568
NM_002185.5(IL7R):c.*1619G>T rs113174267 0.01386
NM_002185.5(IL7R):c.*1508G>C rs111740630 0.01383
NM_002185.5(IL7R):c.*2750C>G rs6885455 0.01076
NM_002185.5(IL7R):c.*508A>G rs74625608 0.01051
NM_002185.5(IL7R):c.*1902C>T rs187393408 0.00780
NM_002185.5(IL7R):c.*42A>G rs145513117 0.00647
NM_002185.5(IL7R):c.*2898G>A rs76863142 0.00469
NM_002185.5(IL7R):c.*453G>T rs79286909 0.00464
NM_002185.5(IL7R):c.1241C>T (p.Thr414Met) rs2229232 0.00456
NM_002185.5(IL7R):c.1231A>G (p.Thr411Ala) rs115316501 0.00398
NM_002185.5(IL7R):c.132C>T (p.Ser44=) rs11567704 0.00357
NM_002185.5(IL7R):c.456A>C (p.Thr152=) rs112805866 0.00130
NM_002185.5(IL7R):c.*2165C>T rs76614394 0.00119
NM_002185.5(IL7R):c.1020T>G (p.Leu340=) rs138731184 0.00096
NM_002185.5(IL7R):c.1188T>C (p.Asn396=) rs145705481 0.00088
NM_002185.5(IL7R):c.1200G>A (p.Val400=) rs140634356 0.00080
NM_002185.5(IL7R):c.*830A>C rs11567769 0.00063
NM_002185.5(IL7R):c.239T>C (p.Val80Ala) rs200475138 0.00055
NM_002185.5(IL7R):c.153G>A (p.Ser51=) rs149235072 0.00035
NM_002185.5(IL7R):c.707G>A (p.Gly236Glu) rs201084372 0.00023
NM_002185.5(IL7R):c.759C>T (p.Val253=) rs201268331 0.00017
NM_002185.5(IL7R):c.283G>A (p.Glu95Lys) rs191585195 0.00005
NM_002185.5(IL7R):c.537+4T>C rs200625485 0.00002
NM_002185.5(IL7R):c.306T>A (p.Ile102=) rs200241281 0.00001
NM_002185.5(IL7R):c.*1253G>A rs10491435
NM_002185.5(IL7R):c.*1253G>T rs10491435
NM_002185.5(IL7R):c.*2568G>T rs6881706
NM_002185.5(IL7R):c.1043A>C (p.Asn348Thr) rs41270321
NM_002185.5(IL7R):c.1092T>G (p.Asp364Glu) rs201216012
NM_002185.5(IL7R):c.876+12del
NM_002185.5(IL7R):c.876+12dup

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.